Data Analyst II, Technical Support - Product Master Data

Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more careers.bms.com/working-with-us.

Position Summary

The person will work on Product Master used across the enterprise. This role is critical to enhance the adoption of tool usage in line with the defined service model across different functions in BMS.

Key Responsibilities

• Contribute as Team Player to deliver assigned PR1ME(Product Information Mastering for the Enterprise) development project(s)
• Participate in analysis of application requirements and provide design ideas to support the business
• Understand the project deliverables and make committed efforts to deliver on intended outcomes
• Identify dependencies, risks, and communicate status to appropriate levels of management and stakeholders across assigned project(s).
• Participate in all aspects of the software development lifecycle which includes estimating, technical design, documentation, deployment, and support
• As a member working in a team environment, you will work with Business team, solution architect, enterprise architects and developers on interpretation/translation of functional requirements into creative designs, leading to technical solution
• Understand and adhere to strong coding standards for efficiency, readability, and reuse
• Strong Technical writing skills for updating supporting documentation, Knowledgebase articles etc.
• Follow Agile development practices for project execution
• 
  Focused effort to resolve the assigned incidents/requests
• Ensure adherence to SOPs and validation best practices

Desired Candidate Characteristics

• Demonstrated Technical Development experience using Stibo technology
• Have a strong commitment to a career in technology with a passion for Pharma/Life sciences industry
• Ability to engage and actively contribute towards team/project success
• Able to collaborate with other team members, across multiple geographies
• Excellent communication skills
• Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo
• Agility to learn new tools and processes

Qualifications & Experience

• Graduate degree in the field of Information Technology or Computer Science from an accredited university
• 3+ years’ experience to design, build, and maintain systems and solve complex master data management operations and automation challenges.

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• 2+ years of experience and in depth knowledge in coding and configuring Stibo STEP, to implement Master Data Management application/s
• Knowledge of Master Data Management and specifically Product Master Data management will be a plus
• Experience in the Biotech/Pharmaceutical Industry and knowledge of working in validated projects will be a plus.
• Experience in using ServiceNow and knowledge of incident/request management will be a plus
• Demonstrates openness to learning and developing. Takes responsibility for their own development and growth.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.